SRX914984 GSM1629373 SRP056007 SRS870008 GSM1629373 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629373 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629373 gds 301629373 GEO Accession GSM1629373 SRX914985 GSM1629374 SRP056007 SRS870007 GSM1629374 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629374 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629374 gds 301629374 GEO Accession GSM1629374 SRX914986 GSM1629375 SRP056007 SRS870006 GSM1629375 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629375 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629375 gds 301629375 GEO Accession GSM1629375 SRX914987 GSM1629376 SRP056007 SRS870005 GSM1629376 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629376 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629376 gds 301629376 GEO Accession GSM1629376 SRX914988 GSM1629377 SRP056007 SRS870004 GSM1629377 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629377 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629377 gds 301629377 GEO Accession GSM1629377 SRX914989 GSM1629378 SRP056007 SRS870002 GSM1629378 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629378 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629378 gds 301629378 GEO Accession GSM1629378 SRX914990 GSM1629379 SRP056007 SRS870001 GSM1629379 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629379 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629379 gds 301629379 GEO Accession GSM1629379 SRX914991 GSM1629380 SRP056007 SRS870003 GSM1629380 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629380 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629380 gds 301629380 GEO Accession GSM1629380 SRX914992 GSM1629381 SRP056007 SRS870000 GSM1629381 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629381 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629381 gds 301629381 GEO Accession GSM1629381 SRX914993 GSM1629382 SRP056007 SRS869999 GSM1629382 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629382 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629382 gds 301629382 GEO Accession GSM1629382 SRX914994 GSM1629383 SRP056007 SRS869997 GSM1629383 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629383 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629383 gds 301629383 GEO Accession GSM1629383 SRX914995 GSM1629384 SRP056007 SRS869998 GSM1629384 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629384 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629384 gds 301629384 GEO Accession GSM1629384 SRX914996 GSM1629385 SRP056007 SRS869995 GSM1629385 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629385 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629385 gds 301629385 GEO Accession GSM1629385 SRX914997 GSM1629386 SRP056007 SRS869996 GSM1629386 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629386 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629386 gds 301629386 GEO Accession GSM1629386 SRX914998 GSM1629387 SRP056007 SRS870009 GSM1629387 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629387 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629387 gds 301629387 GEO Accession GSM1629387 SRX914999 GSM1629388 SRP056007 SRS869994 GSM1629388 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629388 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629388 gds 301629388 GEO Accession GSM1629388 SRX915000 GSM1629389 SRP056007 SRS869992 GSM1629389 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629389 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629389 gds 301629389 GEO Accession GSM1629389 SRX915001 GSM1629390 SRP056007 SRS869993 GSM1629390 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629390 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629390 gds 301629390 GEO Accession GSM1629390 SRX915002 GSM1629391 SRP056007 SRS869991 GSM1629391 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629391 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629391 gds 301629391 GEO Accession GSM1629391 SRX915003 GSM1629392 SRP056007 SRS869990 GSM1629392 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629392 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629392 gds 301629392 GEO Accession GSM1629392 SRX915004 GSM1629393 SRP056007 SRS869989 GSM1629393 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629393 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629393 gds 301629393 GEO Accession GSM1629393 SRX915005 GSM1629394 SRP056007 SRS869988 GSM1629394 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629394 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629394 gds 301629394 GEO Accession GSM1629394 SRX915006 GSM1629395 SRP056007 SRS869987 GSM1629395 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629395 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629395 gds 301629395 GEO Accession GSM1629395 SRX915007 GSM1629396 SRP056007 SRS869986 GSM1629396 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629396 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629396 gds 301629396 GEO Accession GSM1629396 SRX915008 GSM1629397 SRP056007 SRS869985 GSM1629397 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629397 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629397 gds 301629397 GEO Accession GSM1629397 SRX915009 GSM1629398 SRP056007 SRS869984 GSM1629398 ChIP-Seq GENOMIC ChIP For ChIP-seq, samples were fixed for 45 minutes with 2mM DSG followed by 10 minutes with 1% formaldehyde. Fixation was stopped by adding Glycine (0.125M). Chromatin DNA was sheared to 200–500 bp average in size by sonication. Soluble sheared chromatin was immunoprecipitated with specific antibodies coupled with protein G dynabeads (Invitrogen) overnight at 4°C. After washing and elution, the protein–DNA complex was decross-linked by heating at 65°C for 4 hours. Immunoprecipitated DNA was purified by using iPure Diagenode kit. the libraries were constructed following Illumina’s Chip-Seq Sample prep kit. Illumina HiSeq 2000 GEO Sample GSM1629398 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1629398 gds 301629398 GEO Accession GSM1629398